FDA Inspection 683918 — Zoncoarm
The FDA completed an inspection of Zoncoarm on Sep 28, 2010 in Northfield, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 28, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Northfield, MN (United States)